23130[Gene ID] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2324631	NM_015104.3(ATG2A):c.5757T>G (p.Ile1919Met)	ATG2A (I1913M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362744	NM_015104.3(ATG2A):c.5747G>A (p.Arg1916His)	ATG2A (R1910H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299006	NM_015104.3(ATG2A):c.5729G>A (p.Ser1910Asn)	ATG2A (S1902N +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2319381	NM_015104.3(ATG2A):c.5714C>T (p.Thr1905Met)	ATG2A (T1897M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320902	NM_015104.3(ATG2A):c.5710G>A (p.Ala1904Thr)	ATG2A (A1896T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400817	NM_015104.3(ATG2A):c.5687C>T (p.Thr1896Ile)	ATG2A (T1896I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623269	NM_015104.3(ATG2A):c.5672G>A (p.Arg1891His)	ATG2A (R1883H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3321048	NM_015104.3(ATG2A):c.5656G>A (p.Val1886Met)	ATG2A (V1880M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218630	NM_015104.3(ATG2A):c.5648C>G (p.Thr1883Arg)	ATG2A (T1875R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3321011	NM_015104.3(ATG2A):c.5614G>A (p.Val1872Met)	ATG2A (V1864M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363896	NM_015104.3(ATG2A):c.5507G>A (p.Arg1836Gln)	ATG2A (R1836Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2622008	NM_015104.3(ATG2A):c.5506C>T (p.Arg1836Trp)	ATG2A (R1830W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392042	NM_015104.3(ATG2A):c.5492A>T (p.Asp1831Val)	ATG2A (D1825V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511607	NM_015104.3(ATG2A):c.5479C>T (p.Arg1827Cys)	ATG2A (R1821C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 716422	NM_015104.3(ATG2A):c.5473G>A (p.Val1825Ile)	ATG2A (V1817I +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2369522	NM_015104.3(ATG2A):c.5407C>T (p.Arg1803Trp)	ATG2A (R1795W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399218	NM_015104.3(ATG2A):c.5348A>G (p.Gln1783Arg)	ATG2A (Q1783R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130940	NM_015104.3(ATG2A):c.5335A>C (p.Met1779Leu)	ATG2A (M1773L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328916	NM_015104.3(ATG2A):c.5253G>A (p.Met1751Ile)	ATG2A (M1751I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557917	NM_015104.3(ATG2A):c.5116G>C (p.Glu1706Gln)	ATG2A (E1700Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466833	NM_015104.3(ATG2A):c.5050G>A (p.Val1684Ile)	ATG2A (V1676I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315160	NM_015104.3(ATG2A):c.5011T>C (p.Ser1671Pro)	ATG2A (S1663P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540635	NM_015104.3(ATG2A):c.5009C>T (p.Thr1670Met)	ATG2A (T1662M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592178	NM_015104.3(ATG2A):c.4915G>A (p.Val1639Ile)	ATG2A (V1631I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130938	NM_015104.3(ATG2A):c.4862G>A (p.Arg1621His)	ATG2A (R1615H +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2235350	NM_015104.3(ATG2A):c.4831G>A (p.Val1611Met)	ATG2A (V1611M +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2223177	NM_015104.3(ATG2A):c.4819G>A (p.Gly1607Ser)	ATG2A (G1599S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130937	NM_015104.3(ATG2A):c.4738G>A (p.Val1580Ile)	ATG2A (V1574I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130936	NM_015104.3(ATG2A):c.4736G>A (p.Arg1579His)	ATG2A (R1573H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130935	NM_015104.3(ATG2A):c.4586G>A (p.Arg1529Gln)	ATG2A (R1521Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130934	NM_015104.3(ATG2A):c.4567G>A (p.Val1523Met)	ATG2A (V1517M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397236	NM_015104.3(ATG2A):c.4514C>A (p.Ala1505Glu)	ATG2A (A1497E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2641937	NM_015104.3(ATG2A):c.4465-4A>G	ATG2A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3130933	NM_015104.3(ATG2A):c.4412A>G (p.Gln1471Arg)	ATG2A (Q1463R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3321070	NM_015104.3(ATG2A):c.4388G>A (p.Arg1463Gln)	ATG2A (R1463Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3321087	NM_015104.3(ATG2A):c.4385A>C (p.Asn1462Thr)	ATG2A (N1454T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383938	NM_015104.3(ATG2A):c.4370G>A (p.Arg1457His)	ATG2A (R1451H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359819	NM_015104.3(ATG2A):c.4369C>T (p.Arg1457Cys)	ATG2A (R1457C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130932	NM_015104.3(ATG2A):c.4354A>G (p.Arg1452Gly)	ATG2A (R1444G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130931	NM_015104.3(ATG2A):c.4279G>A (p.Val1427Ile)	ATG2A (V1419I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3321077	NM_015104.3(ATG2A):c.4216C>A (p.Leu1406Met)	ATG2A (L1406M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130930	NM_015104.3(ATG2A):c.4168G>A (p.Val1390Ile)	ATG2A (V1384I +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2641938	NM_015104.3(ATG2A):c.4104C>T (p.Pro1368=)	ATG2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2326721	NM_015104.3(ATG2A):c.4100C>T (p.Ala1367Val)	ATG2A (A1367V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3321038	NM_015104.3(ATG2A):c.4027G>C (p.Glu1343Gln)	ATG2A (E1343Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308949	NM_015104.3(ATG2A):c.4007G>A (p.Ser1336Asn)	ATG2A (S1330N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214052	NM_015104.3(ATG2A):c.3973C>G (p.Pro1325Ala)	ATG2A (P1319A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304852	NM_015104.3(ATG2A):c.3958C>T (p.Arg1320Trp)	ATG2A (R1320W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593707	NM_015104.3(ATG2A):c.3901T>C (p.Ser1301Pro)	ATG2A (S1293P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320992	NM_015104.3(ATG2A):c.3883C>T (p.Arg1295Trp)	ATG2A (R1295W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408649	NM_015104.3(ATG2A):c.3875G>A (p.Arg1292His)	ATG2A (R1286H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247529	NM_015104.3(ATG2A):c.3842G>A (p.Arg1281His)	ATG2A (R1273H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538690	NM_015104.3(ATG2A):c.3824C>T (p.Thr1275Met)	ATG2A (T1275M +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2550430	NM_015104.3(ATG2A):c.3814C>G (p.Pro1272Ala)	ATG2A (P1266A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2471633	NM_015104.3(ATG2A):c.3789T>A (p.Ser1263Arg)	ATG2A (S1257R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320939	NM_015104.3(ATG2A):c.3758C>T (p.Thr1253Met)	ATG2A (T1245M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359318	NM_015104.3(ATG2A):c.3743G>C (p.Arg1248Pro)	ATG2A (R1240P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570003	NM_015104.3(ATG2A):c.3737C>G (p.Pro1246Arg)	ATG2A (P1246R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621794	NM_015104.3(ATG2A):c.3736C>A (p.Pro1246Thr)	ATG2A (P1238T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352926	NM_015104.3(ATG2A):c.3709G>A (p.Val1237Ile)	ATG2A (V1229I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510789	NM_015104.3(ATG2A):c.3628G>C (p.Glu1210Gln)	ATG2A (E1210Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590471	NM_015104.3(ATG2A):c.3601G>A (p.Glu1201Lys)	ATG2A (E1201K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290619	NM_015104.3(ATG2A):c.3563T>G (p.Leu1188Arg)	ATG2A (L1180R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245285	NM_015104.3(ATG2A):c.3533G>A (p.Arg1178Gln)	ATG2A (R1178Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130927	NM_015104.3(ATG2A):c.3515A>T (p.Glu1172Val)	ATG2A (E1164V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383618	NM_015104.3(ATG2A):c.3392G>A (p.Arg1131His)	ATG2A (R1123H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130926	NM_015104.3(ATG2A):c.3391C>T (p.Arg1131Cys)	ATG2A (R1131C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2412576	NM_015104.3(ATG2A):c.3307T>C (p.Tyr1103His)	ATG2A (Y1095H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350765	NM_015104.3(ATG2A):c.3283G>A (p.Val1095Met)	ATG2A (V1095M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381591	NM_015104.3(ATG2A):c.3244G>A (p.Glu1082Lys)	ATG2A (E1082K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394179	NM_015104.3(ATG2A):c.3230A>C (p.Tyr1077Ser)	ATG2A (Y1077S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397661	NM_015104.3(ATG2A):c.3203G>A (p.Arg1068Gln)	ATG2A (R1068Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2572303	NM_015104.3(ATG2A):c.3131A>C (p.His1044Pro)	ATG2A (H1036P +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3320982	NM_015104.3(ATG2A):c.3125G>T (p.Gly1042Val)	ATG2A (G1034V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377412	NM_015104.3(ATG2A):c.3092G>A (p.Arg1031Gln)	ATG2A (R1031Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130925	NM_015104.3(ATG2A):c.3058A>G (p.Thr1020Ala)	ATG2A (T1012A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130924	NM_015104.3(ATG2A):c.3041C>T (p.Pro1014Leu)	ATG2A (P1006L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340568	NM_015104.3(ATG2A):c.3025C>T (p.Pro1009Ser)	ATG2A (P1009S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378247	NM_015104.3(ATG2A):c.2992G>C (p.Asp998His)	ATG2A (D998H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2641939	NM_015104.3(ATG2A):c.2989G>A (p.Val997Met)	ATG2A (V989M +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2537425	NM_015104.3(ATG2A):c.2953G>A (p.Glu985Lys)	ATG2A (E977K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320962	NM_015104.3(ATG2A):c.2812A>G (p.Thr938Ala)	ATG2A (T930A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320930	NM_015104.3(ATG2A):c.2807G>A (p.Arg936Gln)	ATG2A (R928Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286668	NM_015104.3(ATG2A):c.2735C>T (p.Ala912Val)	ATG2A (A912V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130922	NM_015104.3(ATG2A):c.2725G>A (p.Gly909Ser)	ATG2A (G901S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466079	NM_015104.3(ATG2A):c.2696C>T (p.Ala899Val)	ATG2A (A899V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320921	NM_015104.3(ATG2A):c.2590G>A (p.Gly864Ser)	ATG2A (G864S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 790099	NM_015104.3(ATG2A):c.2570C>T (p.Ala857Val)	ATG2A (A857V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2515343	NM_015104.3(ATG2A):c.2566G>A (p.Ala856Thr)	ATG2A (A856T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 718557	NM_015104.3(ATG2A):c.2517C>T (p.Asn839=)	ATG2A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3130921	NM_015104.3(ATG2A):c.2473C>G (p.Pro825Ala)	ATG2A (P825A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469603	NM_015104.3(ATG2A):c.2308C>T (p.Arg770Trp)	ATG2A (R770W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2479798	NM_015104.3(ATG2A):c.2237G>T (p.Ser746Ile)	ATG2A (S746I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130920	NM_015104.3(ATG2A):c.2167G>T (p.Asp723Tyr)	ATG2A (D723Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231260	NM_015104.3(ATG2A):c.2150G>A (p.Arg717His)	ATG2A (R717H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245301	NM_015104.3(ATG2A):c.2111T>C (p.Ile704Thr)	ATG2A (I704T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2602612	NM_015104.3(ATG2A):c.2108G>T (p.Gly703Val)	ATG2A (G703V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361667	NM_015104.3(ATG2A):c.2098G>A (p.Asp700Asn)	ATG2A (D700N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468806	NM_015104.3(ATG2A):c.2059G>A (p.Gly687Ser)	ATG2A (G687S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321582	NM_015104.3(ATG2A):c.2042A>G (p.Glu681Gly)	ATG2A (E681G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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